510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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DQHClass II

Cardiograph, Apex (Vibrocardiograph)

21 CFR 870.2310 / Cardiovascular
FDA source (opens on fda.gov)

DQH is the FDA product code for Cardiograph, Apex (Vibrocardiograph), a class II device type, regulated under 21 CFR 870.2310. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DQH
Device name
Cardiograph, Apex (Vibrocardiograph)
Regulation
21 CFR 870.2310
Device class
Class II
Review panel
Cardiovascular
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
1
Ingested recalls
0

Clearances, product code DQH

By decision year
1 clearance under product code DQH with a decision year between 1998 and 1998, 1998 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DQH by decision year
YearClearances
19981

Applicants with the most clearances

Product code DQH
Applicants holding the most 510(k) clearances under product code DQH
ApplicantClearances
Bci Intl., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code